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Venlafaxine - 52125-622-02 - (Venlafaxine)

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Drug Information of Venlafaxine

Product NDC: 52125-622
Proprietary Name: Venlafaxine
Non Proprietary Name: Venlafaxine
Active Ingredient(s): 37.5    mg/1 & nbsp;   Venlafaxine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Venlafaxine

Product NDC: 52125-622
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079009
Marketing Category: ANDA
Start Marketing Date: 20130529

Package Information of Venlafaxine

Package NDC: 52125-622-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-622-02)

NDC Information of Venlafaxine

NDC Code 52125-622-02
Proprietary Name Venlafaxine
Package Description 30 TABLET in 1 BLISTER PACK (52125-622-02)
Product NDC 52125-622
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Venlafaxine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130529
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name VENLAFAXINE HYDROCHLORIDE
Strength Number 37.5
Strength Unit mg/1
Pharmaceutical Classes Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Venlafaxine


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